Organic starch derivatives and process



Patented Feb. 28, 19.39 v

UNITED STATES PATENT OFFICE ORGANIC s'mnon DERIVATIVES AND rnoonss Robert W. Maxwell, Wilmington, DeL, assignmto E. I. du Pont de Nemours & Company, Wilmington, DeL, a corporation of Delaware No Drawing. Application April 15, 1937, Serial No. 137,143

3.5 Claims. (01. 260--209) This invention relates to high viscosity derivatreatment of starch, modified starch or a watertives of starch, more particularly it relates to soluble derivative thereof first with a monofuncderivatives of starch which have been rendered tional agent an t With a bifunctional reagent, of greatly increased viscosity while still remainthe simultaneous treatment of the starch with ing soluble, by the introduction of a very Small a monoand bifunctional reagent, and the treat- 5 amount of a polyfunctional group, still more parment with a bifunctional reagent first and subticularly it relates to the preparation of watersequently with a monofunctional agent. soluble, high viscosity derivatives of starch by the In t e p es t invention bifunctiona-l reagents introduction of a very small amount of a bifunewhich react bifunctionally under the reaction tional etheriflcation or esterification agent. It conditions are used: It is to be emphasized that 10 relates further to the preparation of watercertain reagents which appear to be bifunctlonal soluble high viscosity derivatives of starch by the rea t d n re t s s h without additional introduction of a small amount of a bifunctional rea i n in in ut no catalytic. m n these reagent in connection with precedent, simultameans e g Called n t e art De l5 neous or subsequent treatment of the starch ma- Phth lic anhy r de th s rea s With Star h hyterial with a. monofunctional reagent. In a more droxyls as a monfl reagent. with limited sense, it pertains to the use of said high one hydr xyl up of t star h nu u t viscosity derivatives as thickening agents in the second carboxyl being n tf an imp ll i textile and related arts. It also relates to imus d o ha th s nd x l al o re s. n

proved printing pastes containing said high visinsoluble derivative is formed, or if the amount 20 cosity derivatives of starch, and to process for of P t a anhydridc used s Small d Other preparing the same. solubilizing groups are present, a derivative of This invention has as an object the'production greatly increased viscosity is produced. If a diof high viscosity starch derivatives. A further basic acid is mixed with one mol of benzoyl object is the production of water-soluble high ch d i t p s f py din a d a sta 25 viscosity starch derivatives. Astill further object derivative tr at d with th tur a soluble isthepreparation of starch derivatives of high derivative may be obtained. This is presumably viscosity which are soluble in aqueous solutions because the benzoyl chloride and the dibasic acid and/or organic solvents, and mixtures thereof react to form an intermediate anhydride-acid which may be used commercially throughout the which is monofunctional since it contains only 39 arts as thickening agents. A further object is the On a y e pproduction of high viscosity starch derivatives in commercial quantities. A still further object is fi gggg Co (CHzhCOQH the production of water-soluble starch derivatives which have pronounced adhesive properties. If, however, two mols 0f the benzoyl Chloride 35 oth r objects include t preparation of are used for one mol of the dibasic acid in the proved printing pastes hi give stronger prints presence of pyridine and a starch derivative conand are economical to use. Other objects will taming e 0510 hydroxyls is brought to appear hereinafte g react with it, an ester may he formed in which 40 h above and other bjects may be accomthe starch nucleus is esterified by both carboxyl 40 plished by the following invention wherein starch roups of e c d, a d an insoluble or a modified starch or a water-soluble derivative livative formed; When only Small amounts Of thereof is reacted with a small amount of a polyreagent are used and other Solubilizihg groups functional reagent under such conditions that at e P esent, a product of gre t y increased least two of the functional groups in the same COSitY may be the result Presumably, this is 45 molecule of the reagent react. In a preferred and because the benzoy ch o ide impellor reacts with more limited sense, they are accomplished by rethe dibasic acid to form a di-anhydride which is acting starch, modified starch or a water-soluble polyfunctional because it contains two anhydride derivative. thereof with a small amount of a groups.

bifunctional agent selected from the group con- 2cszhoocl+iiooc orh accord sisting of etherificaticn and esterificatlon agents T and mixtures of the sameincluding mixed ethericemso'o'co'wfiz) fication and esterification agents and mixed I have found that the use of hifunctional reetherification or mixed esterification agents. agents under such conditions that both functional Several variations of the invention include the groups react leads to the formation of high vis- 55 cosity soluble, and even to insoluble derivatives. For example a starch derivative containing tree hydroxyl groups, soluble in solvents when treated with a. biiunctional reagent such as beta, betadichlorodiethyl ether can be rendered completely insoluble in all solvents if the biiunctional reagent is used in large proportions. However, if

the degree of substitution by the biiunctional re- 1 agent is reduced sufliciently either by limiting. the quantity of reagent or the time through which it acts products are obtained which are no longer insoluble but which can be dispersed in the customary solvents for similar starch derivatives containing no bifunctional substituents.

The term soluble and insoluble", as used in this specification, require definition. A starch derivative is described as soluble it it gives a macroscopically homogeneous solution with a quantity of solvent which is more than suflicient to effect maximum swelling. A derivative is said to be insoluble when it can be easily distinguished as a separate phase in the solvent liquid after solute-solvent equilibrium has been attained.

The invention will be further illustrated but is not limited by the following examples in which the quantities are stated in parts by weight.

Example I Sixteen and two-tenths (16.2) parts of potato starch is gelatinized in 94 parts of a 5% aqueous solution of sodium hydroxide by heating on the steam bath for one-halt hour. The mixture is stirred continuously. alkali starch is then cooled to room temperature and 9.2 parts of epichlorohydrin is stirred in. Within fifteen minutes the mixture sets to a rubbery-like gel; This gel is swelled slightly by water but is insoluble in all solvents. i

' Example III mixture is made-of 81 parts of potato starch and 250 parts of water. To this is added 20 parts of sodium hydroxide dissolved in 130 parts of water, and the mixture is heated on a steam bath until the starch has been gelatinized. To the cooled alkali starch solution is added 35.5 parts (0.5 mol) of beta:beta'-dichlorodiethyl ether, with stirring sufiicient to emulsiiy the latter re-. agent in the aqueous solution. The reaction mixture is then maintained at a temperature of 50:5" C. on the steam bath for six hours, with occasional stirring. Samples withdrawn after two and after four hours of the heating period were diluted with water and stirred, with mild warming, until uniformity had' been attained. After cooling, they were neutralized with dilute acetic acid and diluted with an equal volume of methanol to separate the carbohydrate as a rubbery elastic mass. The main portion of the reaction mixture was treated in similar fashion. at the end or six hours heating. The product ob- The uniform mixture of Example IV A mixture was made of 16.2 parts of cornstarch with 32 parts (8 mols) 01 sodium hydroxide dissolved in 48 parts of water by heating and stirring until a uniform mixture resembling a moist clay was obtained. This mixture was transferred to a steam-jacketed Werner-Pileiderer mixer and reacted in the mixer with 57 parts (4 mols) of beta:beta'- dichlorodiethyl ether for 6.5 hours at 82i3 C. v

(as recorded by a thermometer dipped periodically into the reaction mass). The carbohydrate product was separated from the reaction mixture in a manner similar to that given in Example 111 except that the procedure was repeated several times to insure complete removal of sodium salts. The dried product, an amorphous horny mass, was insoluble in all solvents, being swelled to some extent in hot water and aqueous caustic solution. Example V A mixture was made of 16.2 parts of comstarch, 4 parts of sodium hydroxide, and 70 parts of water in a fashion similar to that described in Example 111. This mixture was reacted with 10.7 parts of dichlorodiethyl ether as in Example IV for seven hours at 75:5" 0. The product was obtained as a fine white powder by pouring the cold, neutralized reaction mixture into methanol with violent stirring. The powder was insoluble in all solvents but was swelled in water or aqueous solutions. a 1

Example VI The procedure of'Example V was followed except that 7.1 parts of dichlorodiethyl ether was used instead of 10.7 parts. The product was similar to that obtained in Example V except a slightly greater extent of products obtained in Examples V and VI except that it was swelled to a still greater degree in water. It was insoluble in all solvents.

Example VIII (a) Forty (40) parts of potato starch and 176 parts of water containing dissolved in it 16 parts of sodium hydroxide were mixed to a uniform gelatinous solution by stirring at 70 to 80 C. Forty-seven (47) parts of sodium chloroacetate dissolved in 80 parts. of water were thoroughly stirred into the cooled alkali-starch solution. The resulting mixture was allowed to stand for seventy-two hours at 25 C., with only occasional stirring, and then precipitated in methanol, rinsed with ether and dried in the air.

(b) The dried, powdered product from (a) was dissolved in 250 parts of 20% aqueous sodium hydroxide solution, 17.5 parts of dichlorodiethyl ether were stirred in well, and-the mixture was heated for seven hours at 70 C. After a short heating time, the mixture became quite thick and still. The reaction product, after seven hours heating, was diluted with 1000 parts of water, made just acid to litmus with dilute acetic acid and precipitated by adding methanol. The precipitated product was dehydrated by repeated washings with methanol, filtered, rinsed with, ether, and dried. The product was soluble in water to give very thick solutions much higher in viscosity than the corresponding starch or starch glycolic acid solutions.

Example IX ,(a) One hundred (100) parts of cassava starch are suspended in 250 parts of water and transferred to a steam-jacketed, nickel-lined Werner- Pfieiderer mixer. To this suspension, while being stirred, are added slowly 6.5 parts of caustic soda dissolved in 50 parts of water. At the same time, the temperature of the mixture is raised gradu-- ally to 80 C. When the alkali-starch solution attains uniformity, it is cooled to 30 C. and 10 parts of dimethyl sulfate are worked in gradually. The mixture is stirred one and one-half hours with cooling, heated to 80 C., maintained at 80 C. for fifteen to twenty minutes, tested to confirm alkalinity, cooled and removed from the mixer. The methylated starch is obtained from this solution in the form of a fine white powder by pouring said solution, in a thin stream, into violently agitated methanol, filtering and rinsing the precipitate with acetone or ether before it becomes gummy.

(b) Fifty (50) parts of the powdered product from (a) are treated as in part (b), Example VIII. The product gives with water a very viscous mixture, much higher in viscosity than aqueous dispersions of starch or of the product 1 from (a), a low substituted methyl starch ether.

Example X This illustrates the enhancement of the viscosity of a soluble starch ester by the use of a very small amount of a bifunctional reagent. In this instance the bifunctional reagent is sebacic acid which acts as an esterifying agent for starch hydroxyl groups with both carboxyl groups in the presence of benzoyl chloride and pyridine.

Four and seven-tenths (4.7) parts of starch acetate having an acetic acid' content of 56% were dissolved in 66 parts of pyridine which contained 0.005 part of sebacic acid (one seven hundredth mol of the acid to one mo. of the starch acetate). To this solution 1.75 parts of benzoyl chloride (a considerable excess over two mols for each mol of the acid, the excess being added to take care of moisture in. the material used) were added and stirred in rapidly. The viscosity of the solution increased over a period of twentyfour hours at room temperature until it was about double'the original viscosity and then no further change took place. 'Upon purification and resolution in solvents for starch acetate, the product was found to be soluble and in each case of'in'creased viscosity, usually about double that of the original.

Example XI This illustrates a further increase in viscosity of a starch ester by the use of a slight amount of a bifunctional reagent.

The procedure was exactly the same as in Example X except that 0.009 part of sebacic acid (one four hundredth mol of sebacic acid to each mol of cellulose acetate) was used. The results were the same as in Example X except that the viscosity was approximately four times that of the original instead of twice.

Example XII Example XIII The high viscosity starch derivative prepared according to Example VIII (hereafter designated as starch derivative VIII (is incorporated into a textile printing paste thickener which is formulated as follows:

Parts Starch derivative VIII 6.5 British gum 212.0 Water 441.5 Potassium carbonate 170.0

Sodium sulfoxylate or other reducing agent of the type known to the trade as Rongalit, Hydraldit, Sulfoxite C, etc 120.0 Glycerol 50.0

This printing paste thickener is mixed with a vat dye suitable for dye printing in the proportions:

Parts Vat color 1- 20 Above thickener 99- the precise concentration of dye depending upon the particular dye being used and the depth of color desired in the prints.

Prints made on both rayon and cotton using a paste of the composition above and the vat color known as Sulfanthrene Scarlet G were stronger than similar prints obtained when using a paste formulated as above except that the 6.5 parts of starch derivative VIII were substituted by 32 parts of wheat starch.

Example XIV The procedure of Example IHII was followed except that the printing paste thickener has the following composition: I

. Parts Wheat (or corn) starch 32.0 Starch derivative VIII 8.5 Water 619.5 Potassium carbonate 170.0 Sodium sulfoxylate reducing agent 120.0 Glycerol 50.0

The color printing paste is made by combining tions given in Example XIII.

Example XV The procedure of Example XIII was followed except that the printing paste thickener is formulated as follows:

- Parts 10 .Starch derivative VIII Water v 645 Potassium carbonate -r 1'10 Sodium sulfoxylate reducing agent 120 Glycerol 'l 50 This thickener is incorporated with a vat dye to form a vat color printing paste as in Example XIII.

I Example XVI Starch derivative VIII is incorporated in a printing paste thickener of the following composition:

Parts Starch derivative VIII 20 Gum tragacan Water 900 Glycerol 50 This thickener may be employed for the printing of acid, basic, direct and azoic colors. Ex-

amples of the printing color formulas are:

- (a) Acid colors and direct colors Parts Color 1- 4 Water 19- 16 Above thickener 80 80 (1)) Basic colors Parts 45 Color l- 4 Solvent (alcohol) 5- 10 Acetic acid (glacial) 5- 5 Water 1&- 15 Above thickener d5- 60 50 Tannic-acetic acid (1:1) 6- 6 If maximum brilliancy is preferred, the tanninacetic acid may be eliminated from the above formula.

(c) Azoic colors Example XVII 65 Starch derivative VIII is used as the only thickening agent in a printing paste thickener for the printing of acid, basic, direct and azoic colors. The thickener may have the following composition:

70 I Parts Starch derivative VIII. 30 Water 970 7 This thickener may be substituted in any of oxidized starches (i. e., oxidized with chlorine,

the printing color formulas given in Example xvr Example xvrn The high viscosity starch derivative prepared 5 in Example IX is substituted for starch derivative VIII on an approximately equal weight basis in the formula given inExample XVII. Similarly, it may be used to replace starch derivative VIII in any or all of the formulas given in Ex- 16 amples XIII to XVI.

The viscosity and solubility of starch or starch derivative of any source whatever, provided it contains free hydroxyl groups can be similarly modified by reaction with a bior 'polyfunctional reagent under such conditions that'at least two of the functional groups react. The more familiar starches are corn, wheat, rice, cassava (tapioca), sago, arrow-root, Irish and sweet potato. Modified starches suitable for treatment include hypochlorite, peroxides, perborates, etc.), other kinds of so-called soluble starches, partially -dextrinized starch such as British gum, etc.

Starch ethers, esters and mixed ether-esters, or other substituted derivatives containing unsubstituted hydroxyl groups are susceptible to the described treatment. Among starch derivatives which contain ether groups which render starch water-soluble are methyl and ethyl starch, glycol starch and other hydroxyalkyl starches, and starch glycolic acid. Among useful starch esters are starch acetate, propionate, sulfate, etc. Mixed derivatives such as methyl-ethyl starch, methyl starch acetate, ethyl starch glycolate are also useful. I 85 The term starch material as used in this specification is meant to include'not only the usual types of starches but also chemically modified or soluble starches as well as water-soluble starch derivatives which still contain the starch 40 nucleus, such as starch ethers, esters of organic and inorganic type, ether acids and ether esters. Bifunctional reagents of the etherification and esterification type may be used in accordance with this invention.- In fact, in some instances, triand other polyfunctional reagents may be used in accordance with the teachings of this invention, however, with less satisfaction than when reagents having more than two functional groups are employed. The use of bifunctional etherlflcation' agents represents the preferred embodiment of the invention, As examples of useful agents of this type mention is made of epichlorohydrin, beta:beta-dichlorodiethyl ether and its homologues, beta:beta-dibromdiethyl sulfide, and sulfone. Among useful esterification agents are succinic, adipic, sebacic, phthalic, and other di-basic acids.

The variety of reactions to which this invention is applicable precludes the possibility of setting limits to the reaction conditions of time, temperature, concentrations, etc. Such conditions must be adapted to the type of starch or starch derivative which is submitted to the treatment. and to the particular polyfunctional reagent used. Obviously, some reagents-containing highly reactive functional groups will be eilective at low.

temperatures while others, less reactive, will require elevated temperatures to bring about reaction.

Also, it is quite impossible to specifically define the amount of polyfunctional reagent required. This amount will vary with the polyfunctional reagent used, due to differences in the amounts of such reagents effectively lost in side reactions,

and will depend to some extent upon the desired degree of modification in solubility and viscosity of the starch derivative. It cannot be determined precisely, by present methods of analysis, just how much polyfunctional reagent must react with the starch to produce insolubility, since that amount is usually so small as to be within the limits of experimental error of the analysir The quantity of bifunctional reagent to be used in the reaction can be limited either by controlling the quantities of bifunctional reagent introduced into reaction mass or by limiting the time through which the polyfunctional reagent acts. When the action of monofunctional and polyfunctional reagent takes place simultaneously the quantity of polyfunctional reagent is best regulated by limitation of the amount added. In this case the proper amount can be determined only by running a series of preliminary tests and determining the viscosity and solubility of the resulting products. Where the reaction with the polyfunctional reagent is effected separate from that of a monofunctional reagent the proportion of polyfunctional reagent can be limited either by the quantity of material added to the reaction mixture or the time during which it acts. Wherethe action of the polyfunctional reagent is.to be followed by the action of a monofunctional reagent, or other treatment to improve solubility the proper quantity of polyfunctional reagent to be added or the time through which it acts can be determined only by preliminary tests. If the final product is to be soluble the starch derivative must be of such a nature that it, too, is soluble without the presence of the polyfunctional groups.

The temperature, time and duration of the reaction may vary widely depending upon the particular starch or starch derivative treated, the polyfunctional reagent used, and the amount thereof as Well as the viscosity desired. Obviously, some reagents containing highly reactive functional groups will be effective at low temperatures and others, less reactive, will require elevated conditions. Thus, temperatures from about 15 C. to 120 C. and higher have been found to be useful. Temperatures of 15 C. to 80 C. are, in general, the most practical and are preferred when the reaction is carried out under alkaline conditions.

The amount of polyfunctional reagent used may vary widely, as previously. stated, depending upon its specific nature as well as that of the starch material treated. In some cases, due to side reactions, the eifective amount is considerably below the amount added. In general, it is believed that amounts less than one-fourth of a mol per glucose unit will give soluble derivatives of high viscosity if other conditions are proper. Amounts less than /.20 are in general preferred when alkaline conditions and bifunctional etherification agents are used. By checking the viscosity of the reaction products as the reaction proceeds, the nature of the final product can best be regulated. By following the procedure of the present invention products increased in viscosity from 25 to 1000% or more may be obtained. Best solubility is obtained when the solubility increase is limited from to 400% and preferred products lie within this range.

The products of the present invention have numerous and exceedingly diverse uses in the arts. One important use for high viscosity starch derivatives produced according to the method of the invention is for thickening agents. The products of the invention find numerous other applications as thickeners, for example, in paper printing pastes, agricultural insecticidal sprays, edible jellies, confectionery, ice-cream icings, margarine, mayonnaise, other edible food products, cod-liver oil emulsions, essential oil emulsions, photographic emulsions, cosmetics and toilet preparations, lotions, detergents, polishing and cleaning compositions, adhesives, etc.

The invention has the advantage that starch or a derivative thereof may be given a high viscosity whereby it finds innumerable uses in the arts. It may even be rendered insoluble and resistant to the action of any solvent. It possesses the additional advantages that low molecular weight starch derivatives having low viscosities may be given a high molecular weight and a high viscosity. The products have greater thickening power than starches and may be used towholly or partially replace said thickeners in numerous applications.

Because of their high viscosity, these new starch derivatives may be used at relatively low concentrations and, hence, a smaller amount of thickener is required for a given purpose than when the aforementioned materials are employed. Since the primary function of a thickening agent is to impart increased viscosity to a mixture in which it is incorporated, the advantages of a thickener of extremely high viscosity are readily apparent. Desired thickening action may be secured without using an excessive amount of thickening agent, and in many applications the increasing of the viscosity of a mixture without any appreciable increase in the solids content of said mixture is important. For example, in the printing of textile fabrics, in order successfully to employ the coloring materials a soft thickening material must be added thereto in order to obtain clear and satisfactory printing. After completion of the printing operation, this thickening material must be removed from the fabric and the ease of its removal is an important consideration. It is obvious that the less of such thickening material there is present in the printing paste, the more easily can it be washed out of the fabric. The products of the present invention have superior and unexpected properties in printing pastes and in printing.

A distinct advantage of the starch glycolic acid-beta:beta'-dichlorodiethyl ether reaction product tested as a thickener to replace wheat starch in textile printing pastes, is that the former can be used by merely stirring it into water without heating whereas the latter must be boiled for the preparation of a paste. It has been found that this starch derivative will replace ten parts of wheat starch when used in substantially neutral solutions, and five parts of what starch when used in strongly alkaline solutions.

As many apparently widely different embodi ments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that I do not limit myself to the specific embodiments thereof except as defined in the appended claims.

I claim:

1. The process of producing starch derivatives of high viscosity which comprises reacting a. soluble starch material containing free hydroxyl groups with a small amount of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, and stopping the reaction when a substantial increase in viscosity has been obtained.

2. The process of producing starch derivatives of high viscosity which comprises reacting a soluble starch material containing free hydroxyl groups with a reagent containing from about mol to about 56. mol of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, per glucose unit and stopping the reaction when a substantial increase in viscosity has been obtained.

3. The process of producing starch derivatives of high viscosity which comprises reacting a water-soluble starch material containing free hydroxyl groups with a small amount of bifunctional reagent which reacts with starch through two functional groups of the same molecule of saidgeagent, and stopping the reaction when a substantial increase in viscosity has been obtained and while the product remains water soluble.

4. The process of producing starch derivatives of high viscosity which comprises reacting a water-soluble starch material containing free hydroxyl groups with a reagent containing from about mol to about mol of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, and stopping the reaction when a substantial increase in viscosity has been obtained and while the product remains water soluble.

5. The process of producing starch derivatives of high viscosity which comprises reacting a soluble starch material containing free hydroxyl groups with a small amount of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, taken from the class consisting of etheriflcation and carboxylic acid esteriflcation agents and stopping'the reaction when a pronounced increase in viscosity obtains but before insolubility occurs.

6. The process of producing starch derivatives of increased viscosity which comprises reacting a starch material containing free hydroxyl groups with a small amount of a bifunctional reagent which reacts .with starch through two functional groups of the same molecule of said reagent, and with .a monofunctional reagent said monofunctional reagent being of such a type and present in such a quantity as ordinarily gives a soluble starch derivative and stopping the reaction with the bifunctional reagent when a pronounced increase in viscosity obtains but before insolubility occurs.

'7. The process of producing starch derivatives of increased viscosity which comprises reacting a starch material containing free hydroxyl groups with a small amount'of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, taken from the class consisting of etherification agents and carboxylic acid esteriflcation agents for starch and with a small amount of a monofunctional reagent, the monofunctional reagent being present in such a quantity and being used under such conditions as usually gives a soluble starch derivative and stopping the reaction with the bifunctional reagent at a point at which a pronounced increase in viscosity has been obtained, but before insolubility occurs. 7

8. The process which comprises reacting a starch material containing free hydroxyl groups with a small amount of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, taken from the class consisting of etherification agents and carboxylic acidesterificati'on agents and simultaneously with a monofunctional reagent, the monofunctional reagent being present in such proportions and under such conditions as usually gives a soluble product, the reaction of the bifunctional reagent being stopped when a pronounced increase in viscosity has been obtained but before insolubility occurs.

9. The process which comprises reacting a starch material containing free hydroxyl groups with a small amount of a bifunctional reagent which reacts with starch through two functional groups of the same molecule of said reagent, taken from the class consisting of etherification reagents and carboxylic acid esterification reagents, subsequently reacting the product with a monofunctional reagent in such quantity and in such proportions as usually gives a soluble product, the action of the bifunctional reagent being stopped when a sufiicient degree of reaction has been obtained to render the product of substantially increased viscosity but being stopped before water-insolubility occurs.

10. The process which comprises reacting a starch material containing free hydroxyl groups with a small amount of a monofunctional reagent which reacts with starch through two functional groups of the same molecule of said'reagent, in such quantity and under such conditions as usually gives a water-soluble starch derivative and subsequently with a small amount of a bifunctional reagent taken from the class consisting of etherification agents and carboxylic acid esterificatlon agents and stopping the reaction with the bifunctional reagent when a substantial increase in viscosity has been obtained but before water-insolubility occurs.

11. The process which comprises reacting starch with a small amount of a bifunctional etherification agent which reacts with starch through two functional groups of the same molecule of said agent, and a monofunctional reagent the monofunctional reagent being present in such quantities and being used under such conditions as usually give a soluble starch derivative, the.

action of the bifunctional etherification agent being stopped when a substantial increase in viscosity has been obtained but before insolubility occurs.

12. The process which comprises reacting a water-soluble carboxylic acid ether of starch with a bifunctional etherification agent which reacts with starch through two functional groups of the same molecule of said agent, and stopping the reaction when a substantial increase in viscosity has been obtained but before insolubility' has been obtained.

13. The process which comprises reacting a water-soluble starch ether with a small amount of a bifunctional etherification agent which reacts with starch through two functional groups of the same molecule of said agent, and stopping the reaction when a substantial increase in viscosity has been obtained but beforednsolubility has occurred.

14. As new products, derivatives of starch containing attached to the nucleus, a small amount of a polyfunctional group which is attached to the nucleus at least in part through at least two functional groups.

l5. The.high viscosity water-soluble derivatives of lower aliphatic carboxylic acid ethers of starch containing attached to the nucleus both monofunctional and polyfunctional groups, with the latter attached to the nucleus at least in part, through at least two functional groups.

ROBERT W. MAXWELL.

Patent No. 2,116,951.

' CERTIFICATE OF I CORRECTION.

February 28, 1939. ROBERT w. MAXWELL.

It is hereby'certified'that error appears in .the printed specification of the above numbered patent requiring correction as follows: Page Ll, first colum'n, line 50, for "Tann1c-ace t1c"read Tannin-acetic; page 5, second col- .umn, line 58, for the word "what" read wheat; and that the said Letters Patent should be read with this. correction therein that the same may cenform' to the record of the case in the Patent Office.

Signed and sealed this hth day of April, A. D. 1959.

Henry Van Arsdal e (seal) Acting dommissiener of Patents, 

